Results 21 to 30 of about 161,013 (302)
Spinocerebellar Ataxia Type 2 [PDF]
, 2012 1. Introduction: The autosomal dominant cerebellar ataxias (ADCA) are a clinically, pathologically and genetically heterogeneous group of neurodegenerative disorders caused by degeneration of cerebellum and its afferent and efferent connections.
Auburger, Georg +3 more
core +1 more source
Frontiers in Neurology, 2022 Hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurodegenerative disorders clinically characterized by progressive lower-limb spasticity. Cerebellar ataxia commonly co-occurs with complicated HSPs.
Min-Yu Lan +13 more
doaj +1 more source
IVIG Delays Onset in a Mouse Model of Gerstmann-Sträussler-Scheinker Disease [PDF]
, 2019 Our previous studies showed that intravenous immunoglobulin (IVIG) contained anti-Aβ autoantibodies that might be able to treat Alzheimer's disease (AD).
Dodel, Richard +10 more
core +1 more source
Clinical syndromes associated with Coenzyme Q10 deficiency. [PDF]
, 2018 Primary Coenzyme Q deficiencies represent a group of rare conditions caused by mutations in one of the genes required in its biosynthetic pathway at the enzymatic or regulatory level.
Alc\ue1zar-Fabra, Maria +2 more
core +1 more source
Slow saccades in cerebellar disease [PDF]
Cerebellum & Ataxias, 2019 Eye movements are frequently considered diagnostic markers indicating involvement of the cerebellum. Impaired amplitude of saccades (saccade dysmetria), impaired gaze holding function (horizontal or downbeat nystagmus), and interrupted (choppy) pursuit are typically considered hallmarks of cerebellar disorders.
Jensen, Kelsey +2 more
openaire +2 more sources
Late-onset autosomal recessive cerebellar ataxia and neuropathy with a novel splicing mutation in the ATM gene [PDF]
Journal of Integrative Neuroscience, 2020 Autosomal recessive cerebellar ataxias comprise many types of diseases. The most frequent autosomal recessive cerebellar ataxias are Friedreich ataxia, but other types are relatively rare.
Haruo Shimazaki, Junya Kobayashi, Ryo Sugaya, Imaharu Nakano, Shigeru Fujimoto
doaj +1 more source
SYMPTOMATOLOGY OF CEREBELLAR DISEASE [PDF]
The American Journal of the Medical Sciences, 1895 n ...
openaire +2 more sources
Fractal dimension and variant anatomy of the white matter of the human cerebellar hemisperes
Journal of Education, Health and Sport, 2017 Introduction. Morphological changes of the cerebellar lobules are found in many congenital and acquired diseases of the cerebellum, but the information on the normal structure of the cerebellar lobules do not take into account the peculiarities of ...
N. I. Maryenko, O. Yu. Stepanenko
doaj +3 more sources
Multiple sclerosis: changes in microarchitecture of white matter tracts after training with a video game balance board [PDF]
, 2014 Purpose: To determine if high-intensity, task-oriented, visual feedback training with a video game balance board (Nintendo Wii) induces significant changes in diffusion-tensor imaging (DTI) parameters of cerebellar connections and other supratentorial ...
De Angelis, Floriana +9 more
core +2 more sources